Aminophenylamidines, their production and their medicinal use

ABSTRACT

4-Amino substituted phenylamidine are anthelmintics. The compounds, of which N-(4-aminophenyl)-N&#39;&#39;,N&#39;&#39;-dimethylacetamidine is a representative embodiment, can be prepared through treatment of a 4-amino aniline with a carboxylic acidamide or thioamide, reduction of an appropriately substituted 4-aminophenyl-amidine, optionally followed by alkylation of the resultant 4-aminophenylamidine, formation of a Schiff base followed by quaternization and hydrolysis, or hydrolysis of a 4-acylaminophenylamidine.

United States Patent Wollweber et al.

AMINOPHENYLAMIDINES, THEIR PRODUCTION AND THEIR MEDICINAL USE Inventors: Hartmund Wollweber, Wuppertal,

Germany; Winfried Flucke, Beenleigh, Australia Assignee: Bayer Aktiengesellsehaft, Germany Filed: Oct. 17, 1974 Appl. No: 515,626

Related US. Application Data Division of Ser. No. 399,8l3, Sept. 24, i973, which is a division of Ser No, l5l.575, June 9, 1971, Pat No. 3,855,292.

Foreign Application Priority Data June 13, I970 Germany 202929) [1.8. CI 260/564 RF; 260/5OLI4 Int. Cl. C07C 123/00 Field Of Search .i 260/564 RF, 5(Jl.|4

Dec. 9, 1975 References Cited OTHER PUBLICATIONS Larizza et al., J, Org Chem. Vol 29, pp. 3697-3700 (I964).

Primary Examiner-Gerald A. Schwartz {57] ABSTRACT 3 Claims, N0 Drawings AMINOPHENYLAMIDINES, THEIR PRODUCTION AND THEIR MEDICINAL USE This is a division of Ser. No. 399,813, filed Sept. 24, 1973, which itself is a division of Ser. No. 151,575, filed June 9, 1971, now US. Pat. No. 3,855,292.

DETAILED DESCRIPTION in which:

R is a hydrogen atom or a straightor branched-chain alkyl, alkoxy alkyl or alkenyl group;

R and R are the same or different and are each a hydrogen, fluorine, chlorine or bromine atom or a straightor branched-chain alkyl, alkenyl, or alkoxy group or a cyano or trifluoromethyl group;

R is a straightor branched-chain alkyl or alkenyl group or a cycloalkyl group; and

either R is a straightor branched-chain alkyl, alkenyl or alkoxy group; and

R is a hydrogen atom or a straightor branched-chain alkyl, alkenyl, alkynyl or alkoxy group;

R and R together with the amino nitrogen atom and the amidino carbon atom form a 5, 6 or 7-membered ring;

and their salts.

These aminophenylamidines and -cycloamidines and their non-toxic salts are useful for combating parasites, especially helminths, in human and veterinary medicine.

Alkyl and alkoxy groups R preferably contain 1 to 5, especially l or 2, carbon atoms, and the alkenyl group R preferably contains 2 to 5 carbon atoms.

Alkyl groups R preferably contain 1 to 5, most preferably l or 2, carbon atoms, and alkenyl groups R generally contain 2 to 5, preferably 2 or 3, carbon atoms.

Alkyl and alkoxy groups R and R preferably contain 1 to 6, especially 1 to 3, carbon atoms, and alkenyl groups R and R preferably contain 2 to 6, especially 2 to 4, carbon atoms.

Alkyl and alkoxy groups R preferably contain 1 to 4, especially 1 to 3, carbon atoms. The alkenyl and alkynyl groups R preferably contain 2 to 4 carbon atoms.

If R and R together with the amine nitrogen atom form a S-membered to 7-membered ring, R and R together preferably represent the group (CH,),,-, in which n represents 3, 4 or 5. i

The alkyl groups R preferably contain 1 to 5, especially l to 3, carbon atoms, and the alkenyl groups R preferably contain 2 to 5, especially 2 or 3, carbon atoms. The cycloalkyl group R preferably possesses 3 to 7 carbon atoms.

The active substances according to the invention are basic in character. They can be used as free bases or in the form of their salts, for example hydrohalides, such as, for example, hydrochlorides, sulphates, phosphates, nitrates, acetates, naphthalene disulphonates or pamoates, i.e., the salts with methylene-bis-(Z-hydroxynaphthoic acid-3). The preferred salts are the hydrochlorides.

Particularly preferred compounds are those of the general formula (1) in which:

R is a hydrogen atom or an alkyl or alkylene group containing up to three carbon atoms;

R is a hydrogen, chlorine or bromine atom or a methyl or cyano group;

R is a hydrogen, chlorine or bromine atom or an alkyl group with up to three carbon atoms or a methoxy, trifluoromethyl or cyano group;

R is methyl or ethyl group; and

either R is a methyl or ethyl group or a cycloalkyl group with 3 to 6 carbon atoms; and

R is an alkyl or alkoxy group with l to 3 carbon atoms;

R and R together are a (-CH,+ group, m being a whole number from 3 to 5;

and their salts.

The invention further provides four processes designated as (a), (b), (c) and (d) for the production of the new aminophenylamidines and -cycloamidines and their salts.

Process (a) comprises reacting an aniline derivative of the general formula:

with a carboxylic acid amide or thioamide of the general formula:

or with a salt or a reactive derivative thereof. In general formulae (2) and (3) W is an oxygen or sulphur atom and R, R and R to R are as defined above.

The reaction is optionally carried out in the presence of a condensation agent. The reaction product can be isolated in the form of one of its salts or in the form of a free base, and then optionally converted into any other desired salt.

As salts of the carboxylic acid amides (3) there are to be understood both salts with organic acids, (for examplc, the acetates) and salts with inorganic acids (for example the hydrohalides or sulphates).

By reactive derivatives of the amides (3) there are, for example, to be understood derivatives which are obtained by reaction of an amide or thioamide of the general formula (3) with an inorganic acid (for example, hydrochloric acid, boron trichloride or sulphuric acid) or with an inorganic or organic acid halide (for example, phosphorus oxychloride, phosphorus pentachloride, phosgene, thionyl chloride, benzoyl bromide, p-toluenesulphonyl chloride or a mixture of phosgene/aluminium chloride, or phosgene/hydrogen chloride or phosgene, phosphorus oxychloride) or with a trialkyloxonium fluorborate (l 5 carbon atoms per alkyl group) or with a dialkyl sulphate (1 5 carbon atoms per alkyl group) or an alkyl halide (l 5 carbon atoms).

As condensation agents that can be employed in process (a), there may for example be mentioned:

When a thioamide is used, i.e. W sulphur in general formula (3), a desulphurizing agent, for example, HgO, Ag,0 or Hg(CN can be used advantageously in addition to one of the above-mentioned condensation agents, or without one of these condensation agents.

The reaction components (2) and (3) are preferably employed in the stoichiometrically required amounts.

The reaction can be carried out in any inert organic solvent; among such solvents, aromatic, optionally halogenated, hydrocarbons, for example, benzene, toluene or dichlorobenzene; optionally chlorinated aliphatic hydrocarbons, for example methylene chloride and chloroform; tetramethylene-sulphone, and lower aliphatic alcohols, for example, methanol and ethanol should be mentioned.

The reactants are preferably brought together at room temperature (about 20C) and, if appropriate, are warmed to between 30 and 150C, preferably 80' to 120C, in order to complete the reaction.

The success of the reaction does not depend on the sequence in which the reactants are brought together. The new compounds are isolated in the customary manner.

Process (b) comprises reducing a nitrophenylamidine or -cycloamidine of the general formula:

4 R R R5 5 0221 11:51-14 (4) or a salt thereof, to obtain an aminophenylamidine or -cycloamidine, of the general formula:

i. alkylated with an alkylating agent of the general formula ii. alkylated reductively with an oxo compound of the general formula:

to obtain a Schiff base which is reduced to give the required aminophenylamidine, -cycloamidine or salt.

In the above general formulae (4), (6) and (7), R, R, Rhu 3 to R are as defined above, B is a reactive ester group or a halogen atom; R is a straight-chain or branched alkyl or alkenyl group; R is a hydrogen atom or an alkyl group: and R is an alkyl group.

Straight-chain or branched alkyl groups R' preferably contain 1 to 5 carbon atoms, especially 1 or 2 carbon atoms.

Halogen atoms B are preferably chlorine or bromine 5 atoms. Reactive ester groups B are, for example, arylsulphonyloxy, for example, benzenesulphonyloxy or toxyloxy or alkylsulphonyloxy, for example methanesulphonyloxy, or alkoxysulphonyloxy (preferably with l to 2 carbon atoms in the alkyl or alkoxy group).

5 The alkyl groups R preferably contain 1 to 5, especially l to 4, carbon atoms and the alkyl groups R preferably contain l to 5, especially 1 to 2, carbon atoms. The nitrophenylamidines of general formula (4) and their salts can be reduced by any suitable method.

The reduction can advantageously be effected catalytically, for example with Raney nickel as the catalyst, optionally in the presence of a solvent, such as an alcohol, for example methanol or ethanol, a solution of hydrochloric acid in ethanol, or an ether for example tetrahydrofuran, at a temperature of 0 to C, preferain tetrahydrofuran, at temperatures of 20 to 100C, preferably at the boiling point of the solvent.

Further reducing agents which can be used are complex metal hydrides, such as, for example, sodium boranate in alcohol (preferably ethanol)/water, at temperatures of, preferably, 20 to 80C.

In process (b) (i) l to 2 mols of the alkylating agent of general formula (6) are preferably employed per mol of the intermediate compound Examples of suitable solvents for use in step (i) are water, alcohols, for example, methanol or ethanol, ketones, for example, acetone, ethers for example, tetrahydrofuran, aromatic hydrocarbons, for example, benzene or toluene, or mixtures of these solvents. An increase in the yields can be achieved by the addition of auxiliary bases such as, for example, sodium hydroxide, sodium and potassium carbonate, pyridine or triethylamine.

The reaction is carried out at 0] 00C, preferably at 10 to 40C.

In process (b) (ii) the reactants (5) and (7) are preferably employed in approximately molar amounts. Solvents which can be used for this reaction, which is carried out at 0 to 100C, preferably at about 20 to 60C, are, for example, alcohols, for example, methanol or ethanol, ethers, for example, tetrahydrofuran, and aromatic hydrocarbons, for example, benzene or toluene. The Schiffs base obtained in this manner is hydrogenated, optionally being isolated, by any suitable method. For instance, the base may be catalytically hydrogenated, for example with Raney nickel as the catalyst. The catalytic reduction is preferably carried out at room temperature (about 20C), and optionally under pressure (1 to 80 atmospheres gauge, preferably 60 atmospheres gauge). As a solvent an alcohol, for example methanol and ethanol, an aromatic hydrocarbon, for example, benzene and toluene, or an ether, for example, tetrahydrofuran, can be used.

The reduction of the Schiffs base can also be effected by means of a complex metal hydride (approximately stoichiometrically required amounts), for example, sodium borohydride. [n this case the reaction is carried out at temperatures of 20 to 80C. Here, alcohols, for example methanol and ethanol, optionally in admixture with water, are preferably used as solvents.

Process (c) comprises reacting an aminophenylamidine or -cycloamidine of the general formula:

i.e. a compound of the general formula (I) in which R is hydrogen, with an aliphatic or aromatic aldehyde to obtain a Schiff base quaternising the Schiff base with an alkylastinig agent of the general formula:

acetaldehyde or benzaldehyde, according to any suitable method, to give the Schiff base. The reactants are preferably employed in molar amounts. The reaction temperatures are preferably between 0 and C, preferably between 20 and 40C. Any inert organic solvent may be used, for instance, an alcohol, for example methanol and ethanol, an aromatic hydrocarbon, for example benzene and toluene, or an ether, for example, tetrahydrofuran.

The Schiff base is quaternised, optionally after being isolated, by means of the alkylating agent (6) by any suitable method, preferably at temperatures between 20 to 100C, especially between 60 to 80C. Any inert organic solvent, for example benzene, toluene and tetrahydrofuran can be employed. The subsequent hydrolysis is preferably carried out without isolation of the quaternised Schiff base, preferably at temperatures between 20 to 100C, especially between 40 and C, and preferably in an aqueous alcohol, especially ethanol.

Process (d) comprises hydrolytic splitting of an acylaminophenylamidine or -cycloamidine of the general formula:

in which R, R and R to R are as defined above and R is an acyl or acyloxy group, preferably with l-5 carbon atoms.

The hydrolytic splitting is carried out by any suitable method; many such methods are known in the art.

The hydrolysis is preferably carried out in the presence of a strong acid, such as hydrochloric acid or sulphuric acid. Water, or a mixture of water with an alcohol, is used as a solvent. The hydrolysis is preferably carried out at the boiling point of the solvent.

The following Examples illustrate the process according to the invention for the production of the new aminophenylamidines and cycloamidines.

All temperatures are given in degrees centigrade (C).

All starting compounds are known or are obtainable by known processes.

EXAMPLE I HN N=C-N tract is evaporated, and the residue is distilled in vacuo; the product is N-(4-amino-phenyl)-N',N'-dirnethylacetamidine, boiling point M 158 165, melting point 93 95 (from ethyl acetate); yield 426.5 g, monohydrochloride, melting point 273 274. 5 The following compounds are obtained by analogous processes:

III R VII 1* RV H r: N c N (10) VI IV H,N R' R R" R' R Boiling point] mm Hg 4-NH, H 2-Cl CH, CH, CH, |72/0.3 4-NH, H 3-Cl CH, CH, CH, 17070.3 4-NH, 2-Cl 6-Cl CH, CH, CH, 190/0.s 4-NH, H 2-CH, CH, CH, CH, 175/0.6 4-NH, H 2-0CH, CH, CH, CH, 18070.4 4-NH, H 2-CF, CH, CH, CH, 173'/0.3 4-NH, H 2-CH CH, CH, CH, 168I0.2 4-NH, 2--CN 6-CN CH, CH, CH, 1s4/0.3 4-NH, H Z-Br CH, CH, CH, 1s5/0.4 4-NH, H 2-C,H, CH, CH, CH, 183l0.4 4-NH, H H CH, CH, C,H, l66/0.3 4-NH, H H CH, CH, C,H, l74l03 4-NH, H H CH, C,H, CH, l7l/0.3 4-NH, H H CH, C,H CH, l78/0.3 4-NH, H H C,H, C,H, CH, ism/0a 4-NH, H H H H, CH, |54/0.2 4-NH, H H H C,H, CH, |60l0.2 4-NH, H H H C,H, CH, 168%.: 4-NH, H H H H CH, 4-NH, H H CH, OCH, CH, l63/0.2 4NH, H H CH, OCH, CH, l68/0.2 4-NH, 2--Cl H CH, OCH, CH, 115/0.2

EXAMPLE 2 so The following compounds are produced in accordance with the method described in Example 1, by reduction of 2-(nitro-phenylimino)-azacycloalkanes:

III

C'rl 2 2 N (1 1 IV N B. I

RVI

n H,N R' R R" Boiling noint/ 3 4-NH, H H CH, l'/0.l

Melting point -86 3 4NH, 2Cl H CH, Melting point 9l-92' 3 4-NH, 2-CH, H CH, /0.l 3 4-NH, 2-Br H CH, 20S/0 l 3 4NH, 3-Cl H CH, l93l0v2 3 4-NH, 3-CH, H CH, l92l0.l 3 4NH, 2Cl 6-Cl CH, 210/0.2 3 4NH, 2-CN H CH, l8|/0.2 3 4-NH, H H C,H, I 74/0.2 3 4-NH, 2-Cl H C,H, l88/O.l 4 4-NH, H H CH, 1 7810. l 4 4-NH, 2-Cl H CH, l96l0tl 5 4-NH, 2-Cl H CH, 203/0.l 5 4-NH, H H t CH, l93I0.l 3 4-NH, H H H l78/0.2 3 4-NH, 2-CF, H CH, Melting point 182101 EXAMPLE 3 23 g of isobutyraldehyde are added dropwise, at 20, to 53 g (0.3 mol) of N-(4-aminophenyl)-N',N'-dimethylacetamidine, dissolved in 500 ml of benzene, the mixture is heated for 7 hours whilst connected to a water separator, and the N-(4-isobutylideneaminophenyl)-N,N-dimethylacetamidine is distilled in vacuo; boiling point M l56 160. 8.3 g (0.066 mol) of dimethyl sulphate are added to 13 g (0.056 mol) of this compound, dissolved in ml of benzene, the mixture is heated for 1 hour under reflux, the benzene is decanted off, the residue is taken up in 50 ml of 50% strength ethanol, and the mixture is heated for 1 hour under reflux. After evaporation in vacuo, and treatment of the residue with sodium hydroxide solution, the free base is extracted with ether and distilled: boiling point M l55 hydrochloride, melting point 226 228.

The following compounds are produced by analogous processes:

III RI v11 V N n c N 3) RI/I/ VI RIV R"R'N R'" R R" 12''" RV Boiling point/ mm Hg 4H,CHN 2-Cl H CH, CH, CH, n/0.s 4-H,C-HN Z-Br H CH, CH, CH, l78l0.5 4H,C,HN 2-Cl H CH, CH, CH, l72/0.2 4l-l,C,--HN H H CH, CH, CH, l63/0.5 4H,C,-HN H H CH, CH, CH, [HF/0.6 4- CH,),HC-HN H H CH, CH, CH, l69l0.6 4-H,C-HC=HC-CH,-HN H H CH, CH, CH, l78/0.4 4H,C-HN H H CH, oCH, CH, l62/0.4 4H,C-HN 2-01 H CH, oCH, CH, l78/0.6 4CH, o CH,-CH, HN H CH, CH, CH, l80/0.2

EXAMPLE 4 l5 n R'NH R' R" R" Boiling point/mm Hg 3 4CH NH 2-Cl H CH l9l/0.2 a 4-C,H',-NH 2-Cl H CH: l9B/0.2 3 4-C,H, NH H H CH, |a3/0.3 CH 3 4CH,NH H vH C,H, l86/0.2 a 4-CH,-NH 2-0 H C,H, lag/0.;

4 4-CH -NH H H CH l /0. CH 2 N 4 4CH:-NH 2-CI H CH: 2o2/0.2 s 4-CH,-NH 2-Cl H CH, 212/o.| CH 5 4CH,NH H H CH, |9e/0.2

CH I 3 3 EXAMPLE 6 c ll (14) H N -N N (9) 2 g of the N-(4-isobutylideneaminophenyl)-N',N'- CH dimethylacetamidine obtained according to Example 3, 3 dissolved in 250 ml of tetrahydrofuran, are hydroge- 35 nated with Raney nickel as the catalyst, at 20 50 and 60 atmospheres gauge of hydrogen. After filtering off the catalyst, and distilling, l7.5 g of N-(4- isobutylaminophenyI)-N,N-dimethylacetamidine, boiling point M 138 145, are obtained.

EXAMPLE 5 CH3-NH NQ 1 5) Successive reaction of 2-(4-aminophenyl)-imino-N- methylpyrrolidine with benzaldehyde and dimethyl sulphate, in accordance with the method described in Example 3, yields 2-(4-methylaminophenyl)-imino-N- methylpyrroline, boiling point M 175.

The following compounds are produced in a corresponding way:

25 g of N-(4-carbethoxyaminophenyl)-N,N'-dimethylacetamidine in I00 ml of concentrated hydrochloric acid are heated for 2 hours under reflux. After evaporation, the residue is taken up in water and rendered alkaline with sodium hydroxide solution, and the aqueous phase is extracted with a mixture of ether and chloroform. After distillation, 12 g of N-(4-aminophenyl)- N',N'-dimethylacetamidine, boiling point 158 14 165, melting point 93 14 95, are obtained.

The fact that the new aminophenylamidines and cycloamidines and their salts show a strong and wideranging anthelmintic activity is surprising and unforeseeable.

The new compounds are substantially more effective than other known anthelmintics of the same general action, such as, for example, bephenium hydroxynaphthoates, l,4-phenylene-diisothiocyanate, perchloroethylene, thiabendazole and parbendazole.

Special attention is drawn to the fact that excellent results are achieved with a single administration of the new compounds.

The provision by the invention of these new compounds constitutes a substantial extension of the available range of anthelmintics.

ln particular, the compounds manufactured according to the invention for example display a surprisingly good and broad action against the following helminths (nematodes and cestodes):

l. Nematodes l. Ancylostoma Caninum, Uncinaria srenocephala and Bunostomum trigonocephalum (hookworms) from the family of the Ancylostomatidae;

2. Haemonchus contorrus, Trichosrrongylus colubnformis, Cooperia punctara, Ostertagia circumcincla, Nippostrongylus mun's and Nemalospiroides dubius (worms of the stomach and small intestine) from the family of the Trichostrongylidae;

3. Oesophagostomum columbianum and Chabertia ovina (worms of the large intestine) from the family of the Strongylidae;

4. Strongyloides ram (dwarf threadworms) from the family of the Rhabditidae;

5. Toxocara canis, Toxascaris leom'na and Ascaris suum larvae (coilworms) from the family of the Ascarididae;

6. Aspiculuris letraprem (maggot worms) from the family of the Oxyuridae;

7. Hererakis spumosa from the family of the Heterakidae;

ll. Cestodes 1. Hymenolepis mum and Hymenolepz's microstoma (tapeworms) from the super-family of the Taenioidea.

The action of the new compounds was tested in animal experiments, after oral and parenteral administration to test animals severely infected with parasites. The dosages used were tolerated very well by the test animals.

The unexpected superiority of the compounds according to the invention, as well as their excellent action, is shown by the examples of Tests A D (Tables 1 to 4).

EXAMPLE A Table l Hookworm Test/Dogs Active compounds Dose Action mg/kg in I;

known compounds for comparison:

C H c H -cO-rm-Q -n=c H-N\ .HCl (17) CH CH I 3 3 CI -N=( N (I8) 0 Cl-(i iCl (I9) 300 82 s:C:N--N-(=S 20 so 51 o CH -N CH -CH Q 46 Table lz-continued Hookworm Test/Dogs V Active compounds Dose Action mg/kg in k 3 I l QNSC- C (23) i0 99 Literature: Rawes, D.A. I961):

The activity of Bephenium Hydrocynaphthoate against Hookworms in the Dog Vet.Rec. 73 (16), 390-392 Literature: Theodorides, VJ. and M. Laderman (I968):

Parbendazole in the Treatment of intestinal Nematodes of Dogs and Monkeys. VeLMed. 63 (I0), 985.

EXAMPLE B 25 EXAMPLE C Hookworm Test/Sheep Test on Worm of Large Intestine/Sheep Sheep experimentally infected with Bunostomum Sheep naturally infected with Chabem'a ovina were trigonacephalum were treated after the end of the pretreated after the end of the pre-patent period of the patent period of the parasites. parasites.

The amount of active compound was administered The amount of active compound was administered orally, as pure active compound, in gelatine capsules. orally as pure active compound, in gelatine capsules.

The degree of action was determined by counting the The degree of dilution is determined by counting the worms expelled after the treatment and the worms reworms expelled after the treatment and the worms remaining in the test animals, after dissection, and calcumaining in the test animals, after dissection, and calculating the percentage of worms expelled. 5 lating the percentage of worms expelled.

The active compounds tested, the dosages used and The active compounds tested, the dosages used and the action are shown in the table which follows. the action are shown in the table which follows.

Table 2:

Bookworm Test/Sheep Active compounds Dose Action mg/kg in CH CH Base 2.5 H n -N:-:l 3 (9) am I0 I00 1 Hydrochloride 5 I00 3 "'a H2N 2 "3c-" 29) I0 97 l N 1 (26) 23 s:

Table 3:

Test on Worm of Large Intestine/Sheep Active Compound Dose Action mg/kg in I:

gi /CH n n-4410" 9 1o 97 icine. The eneral sense of the other comments made EXAMPLE 1) g Coilworm Test/Dog Dogs naturally infected with Toxocara cam's or Toxascaris leonina were treated orally. The amount of active compound was administered orally, as pure active compound or as a 10% strength solution in lactic acid, in gelatine capsules.

5 above also applies.

The degree of action is determined by counting the worms expelled after the treatment and the worms remaining in the test animals, after dissection, and calculating the percentage of worms expelled.

The active compounds tested, dosages used and action are summarised in the table which follows.

Table 4:

As stated above, this invention also relates to the pharmaceutical use of the new aminophenylamidines and -cycloamidines and their non-toxic salts,

Accordingly, the present invention provides a pharmaceutical composition containing as an active ingredient at least one of the new aminophenylamidines and -cycloamidines of the general formula l given above, or a non-toxic salt thereof, in admixture with a pharmaceutically acceptable solid or liquid diluent or carrier as hereinafter defined.

In the present specification the expression pharma ceutically acceptable diluent or carrier" means a non- Coilworm Test/Dog Active Compounds Parasite Dose Action mg/kg in C H CH 3 3 Toxocara 2.5 100 2 Toxascaris 5.0 96

C H I 3 cu 3 Toxocara 10.0 60 n NaC- Toxascaris 10.0 s0

In general it has proved advantageous to administer amounts of 0.1 to mg of the new compounds per kg of body weight per day in order to achieve effective results.

Nevertheless it may at times be necessary to deviate from the amounts mentioned, and in particular to do so as a function of the body weight of the test animal or of the nature of the method of administration, but also because of the variety of animal and its individual behaviour towards the medicament or because of the nature of the formulation of the latter and the point in time, or interval, at which it is administered. Thus, it may in some cases suffice to use less than the abovementioned minimum amount, whilst in other cases the upper limit mentioned must be exceeded. Where major amounts are administered, it may be advisable to divide these into several individual administrations over the course of a day. The same dosage range is envisaged for administration in human medicine and in veterinary medtoxic substance that when mixed with the active ingredient or ingredients renders it suitable for administration. The expression preferably excludes water and low-molecular weight organic solvents commonly used in chemical synthesis, except in the presence of other pharmaceutically necessary ingredients such as salts in correct quantities to render the composition isotonic, buffers, surfactants, colouring and flavouring agents, and preservatives. Examples of suitable liquid and solid diluents and carriers are the following:

Buffered aqueous solutions; isotonic saline aqueous solutions; non-toxic organic solvents; such as paraffins, (for example petroleum fractions); vegetable oils (for example groundnut and sesame oils); alcohols, (for example ethyl alcohol or glycerol); glycols (for example propylene glycol or polyethylene glycol); solid excipients, for example, natural ground rock (for example kaolins, aluminas, talc or chalk), synthetic rock powders (for example highly disperse silica or silicates); and sugars (for example unrefined sugar, lactose and 19 glucose). Examples of pharmaceutical compositions according to the invention are ointments, pastes, creams, sprays, lotions, aqueous suspensions, emulsions and solutions, elixirs, syrups, granules and powders, either free-flowing or compressed into tablets.

The compounds and pharmaceutically acceptable salts of the present invention may be administered perorally.

One group of preferred pharmaceutical compositions of the invention are therefore those adapted for oral administration. The diluents and carriers used are preferably therefore those that adapt the active ingredient or ingredients for oral administration. Examples of such diluents and carriers are solid vehicles, excipients and lubricants such as glucose, lactose and sucrose, corn and potato starch, sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate, powdered gum tragacanth, gelatin, alginic acid, agar, stearic acid, sodium, calcium and magnesium stearates, sodium lauryl sulphate, sodium citrate, calcium carbonate, and dicalcium phosphate.

The pharmaceutical compositions of the invention may also contain other non-toxic adjuvants and modifiers such as dyes, surfactants, for example, emulsifiers, such as non-ionic and anionic emulsifiers (for example polyoxyethylene-fatty acid esters, polyoxyethylenefatty alcohol ethers, alkylsulphonates and arylsulphonates), and dispersing agents (for example lignin, sulphite waste lyes, methylcellulose, starch and polyvinylpyrrolidone), perfumes, flavouring agents, preservatives and biocides.

The compounds and pharmaceutically acceptable salts of the invention may also be administered parenterally, in particular subcutaneously. A group of preferred pharmaceutical compositions of the invention are therefore those adapted for parenteral injection. The diluents and carriers used are therefore preferably those that adapt the active ingredient for parenteral administration. Examples of such diluents and carriers are solvents and suspending diluents such as water and water-miscible organic solvents, in particular sesame oil, groundnut oil, aqueous propylene glycol, and N,N'- dimethyl formamide. Examples of pharmaceutical compositions of the invention are sterile isotonic saline aqueous solutions of the active ingredient, which may be buffered with a pharmaceutically acceptable buffer and are preferably pyrogen-free.

The pharmaceutical compositions of the invention generally contain 0.5 to 90 wt. of a new aminophenylamidine or -cycloamidine of the invention or a non'toxic salt thereof.

The present invention also provides medicaments in dosage unit form as hereinafter defined comprising as an active ingredient at least one aminophenylamidine or -cycloamidine of general formula l given above or a non-toxic salt thereof, either alone or in admixture with a pharmaceutically acceptable solid or liquid diluent or carrier. in this case the diluent or carrier is preferably as defined above but can also be water or another common solvent.

The expression medicament in dosage unit form" as used in the present specification means a medicament in the form of discrete portions each containing a unit dose or a multiple or sub-multiple of a unit dose of the active ingredient(s); for example, 1, 2, 3 or four unit doses or a half, a third or a quarter of a unit dose. A unit dose is the amount of the active ingredient(s) to be administered on one occasion and will usually be a LII daily dose, or for example a half, a third, or a quarter of a daily dose depending on whether the medicament is to be administered once or, for example, twice, three times, or four times a day.

The discrete portions constituting the medicament in dosage unit form can include a protective envelope. The active ingredient can be undiluted and contained in such an envelope, or can be mixed with a pharmaceutically acceptable solid or liquid diluent or carrier as defined above. Such portions can for example be in monolithic coherent form, suc as tablets, lozenges, pills, suppositories, or dragees; in wrapped or concealed form, the active ingredients being within a protective envelope, such as wrapped powders, cachets, sachets, capsules, or ampoules; or in the form of a sterile solution suitable for parenteral injection, such as ampoules of buffered, isotonic, sterile, pyrogen-free aqueous solution; or in any other form known in the art.

As stated above, it is preferred to administer the new aminophenylamidines and -cycloamidines of general formula (I) or their salts perorally. Preferred medicaments in dosage unit form according to the invention are therefore those adapted for oral administration, such as tablets, pills dragees, capsules, and cachets, as well as wrapped powders containing the active ingredient in powdered form with a powdered diluent or carrier for suspension in water before being taken.

As stated above it is also possible to administer the new aminophenylamidines and -cycloamidines parenterally. A further group of medicaments in dosage unit form according to the invention are therefore those adapted for parenteral injection, such as ampoules containing a measured quantity of a sterile isotonic saline injectable aqueous solution of the new active ingredient, which may be buffered with a pharmaceutically acceptable buffer and are preferably free of pyrogens.

The preferred unit dose for administration of the medicaments of the invention is 50 2,250 mg. of active ingredients. This will normally be administered once daily.

The invention further provides a method of combating parasitic infestation in an animal which comprises administering to the animal (preferably parenterally or perorally) an aminophenylamidine or -cycloamidine or a non-toxic salt thereof, a pharmaceutical composition or a medicament in dosage unit form according to the invention.

The administration is preferably carried out orally, but may also be carried out parenterally, in particular subcutaneously.

What we claim is:

1. A compound of the formula:

1 5 R NH- N-C R wherein R is hydrogen, alkyl of l to 5 carbon atoms, alkoxyalkyl of 2 to 5 carbon atoms or alkenyl of 2 to 5 carbon atoms;

22 or a salt thereof ofa pharmaceutically acceptable acid. 2. A compound according to claim 1 wherein R is alkyl.

3. A salt of a compound of claim 1 wherein said salt is selected from the group consisting of hydrohalides, sulphates, phosphates, nitrates, acetates, naphthalene disulphonates and pamoates. 

1. A COMPOUND OF THE FORMULA:
 2. A compound according to claim 1 wherein R5 is alkyl.
 3. A salt of a compound of claim 1 wherein said salt is selected from the group consisting of hydrohalides, sulphates, phosphates, nitrates, acetates, naphthalene disulphonates and pamoates. 